2016
DOI: 10.1016/j.ympev.2016.04.035
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Species delimitation and phylogenetic relationships in a genus of African weakly-electric fishes (Osteoglossiformes, Mormyridae, Campylomormyrus)

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Cited by 29 publications
(46 citation statements)
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“…Given the phylogeny of the Campylomormyrus genus and of the African weakly electric fish in general, short snouts are considered ancestral. In fact, most Campylomormyrus species (including the basal C. tamandua) and many other mormyrid species (including Gnathonemus, the sister taxon of Campylomormyrus) display short snouts (Lamanna et al 2016). Only species of one derived lineage, i.e., C. rhynchophorus, C. numenius, and C. curvirostris, have evolved very long snouts (Feulner et al 2007;Lamanna et al 2016).…”
Section: Discussionmentioning
confidence: 99%
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“…Given the phylogeny of the Campylomormyrus genus and of the African weakly electric fish in general, short snouts are considered ancestral. In fact, most Campylomormyrus species (including the basal C. tamandua) and many other mormyrid species (including Gnathonemus, the sister taxon of Campylomormyrus) display short snouts (Lamanna et al 2016). Only species of one derived lineage, i.e., C. rhynchophorus, C. numenius, and C. curvirostris, have evolved very long snouts (Feulner et al 2007;Lamanna et al 2016).…”
Section: Discussionmentioning
confidence: 99%
“…One should also take into consideration the phylogenetic framework of our study. In fact, C. compressirostris and C. rhynchophorus are closely related, while the short snouted C. tamandua stands phylogenetically apart (Lamanna et al 2016). As C. compressirostris and C. rhynchophorus are closely related and significantly differ in both snout length and substrate preference, divergent snout evolution in an ecological speciation context seems a plausible scenario for these species (Feulner et al 2008;Tiedemann et al 2010), while further adaptations may have contributed to the divergence of the more distant lineages.…”
Section: Discussionmentioning
confidence: 99%
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“…(, ) presented genus‐level molecular phylogenies covering 20 of the 22 mormyroid genera. Additionally, species‐level molecular phylogenies have been published for several of the high‐diversity mormyroid genera, including Campylomormyrus : (Feulner et al ., ; Lamanna et al ., ; Tiedemann et al ., ), Marcusenius (Kramer et al ., ), Paramormyrops (Arnegard et al ., ; Rich et al ., ; Sullivan et al ., , ), Petrocephalus (Lavoué, , ) and Pollimyrus (Kramer et al ., ). Species‐level molecular phylogenetic reconstructions covering the entire gymnotiform order have recently become available (Janzen, ; Tagliacollo et al ., ) and species‐level molecular phylogenies including additional diversity are available for two high‐diversity genera: Brachyhypopomus (Crampton et al ., ) and Gymnotus (Brochu, ; Lovejoy et al ., ).…”
Section: Signal Evolution and Sensory Ecology In Mormyroid And Gymnotmentioning
confidence: 99%
“…In both cases, the neofunctionalisation involved one of two paralogues of the scn4aa gene that originated from a whole-genome duplication event prior to the diversification of teleosts . Arnegard et al (2010b) demonstrated that the co-option is tightly coupled to the two convergent origins of electric organs and showed that during subsequent The superfamily Mormyroidea, which is restricted to tropical and subtropical Africa, comprises 229 species belonging to two families and 22 genera (Eschmeyer et al, 2018;Sullivan, 2018 (Feulner et al, 2008;Lamanna et al, 2016;Tiedemann et al, 2010),…”
Section: On the Origins Of Electric Organsmentioning
confidence: 99%